1.3.6.1.4.1.19376.1.5.3.1.1.16.5.4: Difference between revisions
Jump to navigation
Jump to search
m New page: {{V|1.3.6.1.4.1.19376.1.5.3.1.1.16.5.4|Name|Opt|Type|Units|SNOMED CT|LOINC|Title=APR H&P Family History and Genetic Screening Observation Codes|Rows= {{R|Thalassemia |R|CD| |40108008|... |
Tsoutherland (talk | contribs) No edit summary |
||
| Line 1: | Line 1: | ||
{{V|1.3.6.1.4.1.19376.1.5.3.1.1.16.5.4|Name|Opt|Type|Units|SNOMED CT|LOINC|Title=APR H&P Family History and Genetic Screening Observation Codes|Rows= | {{V|1.3.6.1.4.1.19376.1.5.3.1.1.16.5.4|Name|Opt|Type|Units|SNOMED CT|LOINC|Title=APR H&P Family History and Genetic Screening Observation Codes|Rows= | ||
{{R|Thalassemia | {{R|Thalassemia | ||
| | |R2|CD| |40108008|}} | ||
{{R|Neural Tube Defect | {{R|Neural Tube Defect | ||
| | |R2|CD| |253098009|}} | ||
{{R|Congenital Heart Defect | {{R|Congenital Heart Defect | ||
| | |R2|CD| |13213009|}} | ||
{{R|Down Syndrome | {{R|Down Syndrome | ||
| | |R2|CD| |41040004|}} | ||
{{R|Tay-Sachs | {{R|Tay-Sachs | ||
| | |R2|CD| |111385000|}} | ||
{{R|Canavan Disease | {{R|Canavan Disease | ||
| | |R2|CD| |80544005|}} | ||
{{R|Familial Dysautonomia | {{R|Familial Dysautonomia | ||
| | |R2|CD| |29159009|}} | ||
{{R|Sick Cell Disease | {{R|Sick Cell Disease | ||
| | |R2|CD| |417357006|}} | ||
{{R|Sick Cell Trait | {{R|Sick Cell Trait | ||
| | |R2|CD| |16402000|}} | ||
{{R|Hemophilia | {{R|Hemophilia | ||
| | |R2|CD| |90935002|}} | ||
{{R|Blood Disorders | {{R|Blood Disorders | ||
| | |R2|CD| |414022008|}} | ||
{{R|Muscular Dystrophy | {{R|Muscular Dystrophy | ||
| | |R2|CD| |73297009|}} | ||
{{R|Cystic Fibrosis | {{R|Cystic Fibrosis | ||
| | |R2|CD| |190905008|}} | ||
{{R|Huntington's Chorea | {{R|Huntington's Chorea | ||
| | |R2|CD| |58756001|}} | ||
{{R|Mental Retardation | {{R|Mental Retardation | ||
| | |R2|CD| |91138005|}} | ||
{{R|Autism | {{R|Autism | ||
| | |R2|CD| |408856003|}} | ||
{{R|Chrosomosal Disorder<br/>Includes any inherited genetic or chromosomal disorders| | {{R|Chrosomosal Disorder<br/>Includes any inherited genetic or chromosomal disorders | ||
|R2|CD| |409709004|}} | |||
{{R|Maternal Metabolic Disorder | {{R|Maternal Metabolic Disorder | ||
| | |R2|CD| |75934005|}} | ||
{{R|Dysmorphism (Birth Defect)<br/>Patient or baby's father has a child with birth defects| | {{R|Dysmorphism (Birth Defect)<br/>Patient or baby's father has a child with birth defects | ||
|R2|CD| |276720006|}} | |||
{{R|Recurrent pregnancy loss/stillbirth | {{R|Recurrent pregnancy loss/stillbirth | ||
| | |R2|CD| |102878001|}} | ||
}} | }} | ||
Latest revision as of 10:54, 18 September 2008
APR H&P Family History and Genetic Screening Observation Codes Value Set 1.3.6.1.4.1.19376.1.5.3.1.1.16.5.4
| Name | Opt | Type | Units | SNOMED CT | LOINC |
|---|---|---|---|---|---|
| Thalassemia | R2 | CD | 40108008 | ||
| Neural Tube Defect | R2 | CD | 253098009 | ||
| Congenital Heart Defect | R2 | CD | 13213009 | ||
| Down Syndrome | R2 | CD | 41040004 | ||
| Tay-Sachs | R2 | CD | 111385000 | ||
| Canavan Disease | R2 | CD | 80544005 | ||
| Familial Dysautonomia | R2 | CD | 29159009 | ||
| Sick Cell Disease | R2 | CD | 417357006 | ||
| Sick Cell Trait | R2 | CD | 16402000 | ||
| Hemophilia | R2 | CD | 90935002 | ||
| Blood Disorders | R2 | CD | 414022008 | ||
| Muscular Dystrophy | R2 | CD | 73297009 | ||
| Cystic Fibrosis | R2 | CD | 190905008 | ||
| Huntington's Chorea | R2 | CD | 58756001 | ||
| Mental Retardation | R2 | CD | 91138005 | ||
| Autism | R2 | CD | 408856003 | ||
| Chrosomosal Disorder Includes any inherited genetic or chromosomal disorders |
R2 | CD | 409709004 | ||
| Maternal Metabolic Disorder | R2 | CD | 75934005 | ||
| Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects |
R2 | CD | 276720006 | ||
| Recurrent pregnancy loss/stillbirth | R2 | CD | 102878001 |